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Skinbutak Go Young Magiclotion

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This product has been discontinued

Active ingredient
Glycerin 1.4 mg/100 mL
Other brand names
Dosage form
Lotion
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2021
Label revision date
April 26, 2021
Active ingredient
Glycerin 1.4 mg/100 mL
Other brand names
Dosage form
Lotion
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2021
Label revision date
April 26, 2021
Manufacturer
NatureBlue Co. , Ltd
Registration number
part334
NDC root
81851-201

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If you are a consumer or patient please visit this version.

Drug Overview

SKINBUTAK GO YOUNG MAGIC LOTION is a topical product designed for application on the skin. It comes in a 120ml bottle and is intended to help improve the appearance of your skin. By applying the lotion evenly, you can benefit from its skin-enhancing properties, which may contribute to a more youthful look.

Uses

You can use this product by applying an appropriate amount evenly to your skin. It's designed for topical use, meaning it works directly where you apply it.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects associated with this product. This makes it a safe option for your skincare needs.

Dosage and Administration

To achieve soft, brighter, and revitalized skin, you should follow a consistent skincare routine that includes the appropriate products for your skin type. It's important to apply these products regularly to see the best results.

Start by cleansing your skin to remove any dirt and impurities. After cleansing, apply a moisturizer or treatment that is designed to enhance skin brightness and vitality. Make sure to use these products as directed, typically once or twice daily, to maintain the health and appearance of your skin. Consistency is key, so stick to your routine for the best outcome.

What to Avoid

You should avoid applying this product to any wounds or damaged skin, as it can cause irritation or complications. Additionally, do not bandage the area tightly, as this can restrict blood flow. It's also important to keep the product away from your eyes to prevent discomfort or injury. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

It's important to use this product only on the skin and avoid swallowing it. If you accidentally swallow it, seek medical help or contact a Poison Control Center right away.

You should stop using the product and consult your doctor if your condition worsens, if symptoms last more than seven days, or if symptoms improve and then return within a few days. Additionally, do not apply it to wounds or damaged skin, and avoid tightly bandaging the area where it is applied.

Warnings and Precautions

This product is for external use only. If you accidentally swallow it, seek medical help or contact a Poison Control Center right away.

You should stop using this product and consult your doctor if your condition worsens, if your symptoms last more than 7 days, or if your symptoms improve and then return within a few days. Avoid applying it to wounds or damaged skin, and do not wrap the area tightly with a bandage.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help right away. You can contact a Poison Control Center for guidance on what to do next.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to get help immediately. Remember, acting quickly can make a significant difference in ensuring safety and health.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that the effects of the medication on you and your developing baby are not well understood.

If you are pregnant or planning to become pregnant, it’s important to discuss any medications you are taking with your healthcare provider. They can help you weigh the potential risks and benefits to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the use of this medication during nursing. This means that the effects on breast milk and your baby are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding. They can help you weigh the potential risks and benefits to ensure the safety of both you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children. This precaution helps prevent accidental ingestion, which can be dangerous. Always store it in a safe place where children cannot access it, ensuring their safety at all times. If you have any concerns about how to manage medications in your home, don't hesitate to ask your healthcare provider for guidance.

Geriatric Use

When it comes to using SKINBUTAK GO YOUNG MAGICLOTION, there is no specific information available about how it may affect older adults. This means that there are no special dosage adjustments, safety concerns, or precautions outlined for elderly patients.

If you are an older adult or a caregiver, it's always a good idea to consult with a healthcare professional before starting any new treatment. They can provide personalized advice based on individual health needs and conditions.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (issues with liver function).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that your treatment is safe and effective based on your individual health needs.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, always ensure that your healthcare provider is aware of all the medications you are using, as this helps them provide the best care tailored to your needs.

By discussing your full medical history and any other treatments, you can help prevent potential issues and ensure your safety.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. This helps maintain its effectiveness and safety. When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage.

If you have any components that come with the product, make sure to keep them in a clean and safe environment. Proper storage and careful handling are key to ensuring that everything works as intended.

Additional Information

You will apply this medication topically, which means you will apply it directly to the skin. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or experiences reported after the medication has been on the market.

FAQ

What is SKINBUTAK GO YOUNG MAGIC LOTION used for?

SKINBUTAK GO YOUNG MAGIC LOTION is used for achieving soft, brighter, and revitalized skin.

How should I use SKINBUTAK GO YOUNG MAGIC LOTION?

Take an appropriate amount and apply it evenly to the skin.

Are there any contraindications for using this lotion?

Do not apply SKINBUTAK GO YOUNG MAGIC LOTION to wounds or damaged skin, and do not bandage tightly.

What should I do if I accidentally swallow the lotion?

If swallowed, get medical help or contact a Poison Control Center immediately.

What should I do if my condition worsens while using the lotion?

Stop use and ask a doctor if your condition worsens or if symptoms last more than 7 days.

Is SKINBUTAK GO YOUNG MAGIC LOTION safe to use during pregnancy?

No specific information regarding safety during pregnancy is provided in the insert.

Can I use this lotion while breastfeeding?

No specific information regarding use during lactation is provided in the insert.

How should I store SKINBUTAK GO YOUNG MAGIC LOTION?

Store SKINBUTAK GO YOUNG MAGIC LOTION at room temperature.

Is this lotion for external use only?

Yes, SKINBUTAK GO YOUNG MAGIC LOTION is for external use only.

What should I do if the lotion gets into my eyes?

Avoid getting SKINBUTAK GO YOUNG MAGIC LOTION into your eyes.

Are there any known drug interactions with this lotion?

No drug interactions were mentioned in the provided text.

Is there any information about the use of this lotion in elderly patients?

No specific information regarding geriatric use or safety concerns for elderly patients is provided.

Packaging Info

Below are the non-prescription pack sizes of Skinbutak Go Young Magiclotion (glycerin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Skinbutak Go Young Magiclotion.
Details

Drug Information (PDF)

This file contains official product information for Skinbutak Go Young Magiclotion, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product is identified as SKINBUTAK GO YOUNG MAGIC LOTION, with an SPL Code of 34089-3. It is available in a packaging size of 120 ml.

Uses and Indications

This drug is indicated for topical application to the skin. An appropriate amount should be taken and applied evenly to the affected area.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

For optimal results in achieving soft, brighter, and revitalized skin, the recommended dosage and administration should be tailored to the individual patient's needs.

Healthcare professionals should assess the patient's skin condition and determine the appropriate formulation and concentration. The product should be applied topically to the affected areas of the skin.

The application frequency may vary based on the specific formulation used, but it is generally advised to apply the product once or twice daily. Patients should be instructed to cleanse the skin thoroughly before application to enhance absorption and efficacy.

In cases where the product is a cream or lotion, a pea-sized amount should be sufficient for each application. For serums or concentrated formulations, a few drops may be adequate.

It is essential to monitor the patient's response to treatment and adjust the frequency or amount of application as necessary to achieve the desired results while minimizing potential irritation.

Contraindications

Application of this product is contraindicated in the following situations:

  • Do not apply to wounds or damaged skin due to the risk of irritation and impaired healing.

  • Do not bandage tightly, as this may restrict circulation and lead to complications.

  • Avoid contact with eyes to prevent irritation or injury.

Warnings and Precautions

For external use only. In the event of accidental ingestion, it is imperative to seek medical assistance or contact a Poison Control Center immediately.

Healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or symptoms resolve and then recur within a few days. It is crucial to avoid application on wounds or damaged skin, and patients should be instructed not to apply a tight bandage over the treated area.

Side Effects

Patients should be aware that the product is intended for external use only. In the event of accidental ingestion, it is imperative to seek medical assistance or contact a Poison Control Center immediately.

Participants are advised to discontinue use and consult a healthcare professional if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or symptoms resolve and then recur within a few days. Additionally, the product should not be applied to wounds or damaged skin, and it is important to avoid tight bandaging of the area where the product is applied.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Skinbutak Go Young Magiclotion (glycerin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Skinbutak Go Young Magiclotion.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. It is essential to ensure that the medication is stored safely to prevent accidental ingestion or misuse.

Geriatric Use

There is no specific information regarding the use of SKINBUTAK GO YOUNG MAGICLOTION in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this product to elderly patients, as the absence of data necessitates careful consideration of individual patient factors and potential risks. Monitoring for any adverse effects is advisable in this population, given the lack of established guidelines for geriatric use.

Pregnancy

There is no specific information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of informing their healthcare provider if they become pregnant or plan to become pregnant while using this medication.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or any lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. Further research may be necessary to fully understand the implications for breastfed infants.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there are no established dosage adjustments, special monitoring requirements, or precautions outlined for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be prudent in these cases, although specific parameters are not defined in the available information.

Overdosage

In the event of an overdosage, it is imperative that immediate medical assistance is sought. Healthcare professionals should advise patients or caregivers to contact a Poison Control Center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved; however, it is crucial to monitor the patient closely for any signs of adverse reactions. Prompt recognition of symptoms can facilitate timely intervention and management.

Management of overdosage should be guided by the severity of symptoms and the specific circumstances surrounding the incident. Healthcare providers are encouraged to follow established protocols for the assessment and treatment of overdosage cases, which may include supportive care and symptomatic treatment as necessary.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are available for the product associated with SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients to keep the product out of reach of children to prevent accidental ingestion or misuse. Patients should be instructed to stop using the product and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, patients should be informed to seek medical advice if symptoms improve and then recur within a few days.

It is important to emphasize that the product should not be applied to wounds or damaged skin, as this may lead to adverse effects. Patients should also be cautioned against tightly bandaging the area where the product is applied, as this could exacerbate potential side effects. Furthermore, healthcare providers should remind patients to avoid contact with the eyes while using the product, as this may cause irritation or other complications.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at room temperature to maintain its integrity and efficacy. No special handling requirements are noted; however, standard precautions should be observed to ensure optimal storage conditions.

Additional Clinical Information

The route of administration for the medication is topical. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Skinbutak Go Young Magiclotion, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Skinbutak Go Young Magiclotion, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.