Label: SALICYLIC ACID COTTON SHEET- anti acne cotton tablets tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 81950-001-01 - Packager: Pang's International Holdings Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated May 25, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
avoid contact with eyes.If product gets into eyes, rinse thoroughly with water.
skin irritation and dryness is more likely to occur if you use another topical acne medication at the sametime.lf irritation occurs, onlyy use one topical acne medication at a time.
limit use to the face and neck.Stop use and ask a doctor if skin or eye irritation develops.
Keep out of reach of children.If swallowed, get medical help or contact Poison Control Center immediately.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
clean the skin thoroughly before applying this product.
wipe a pad over face and neck to cover the entire affected area with a thin layer one to three times daily.
because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
if bothersome dryness or peeling occur, reduce application to once a day or every other day. - Other information
- Inactive ingredients
- Questions
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID COTTON SHEET
anti acne cotton tablets tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81950-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V) SODIUM HYDROXIDE (UNII: 55X04QC32I) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) CISTUS MONSPELIENSIS LEAF (UNII: 1IE70KNO43) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) LAVANDULA STOECHAS WHOLE (UNII: MTZ2ZA34ZV) HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24) GLYCERIN (UNII: PDC6A3C0OX) ISOCETETH-20 (UNII: O020065R7Z) WATER (UNII: 059QF0KO0R) Product Characteristics Color white Score no score Shape ROUND Size 65mm Flavor FRUIT (Alcohol and melon) Imprint Code no Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81950-001-01 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/30/2020 Labeler - Pang's International Holdings Limited (552701644) Registrant - Pang's International Holdings Limited (552701644) Establishment Name Address ID/FEI Business Operations Pang's International Holdings Limited 552701644 manufacture(81950-001)
