Label: PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL- salicylic acid liquid
- NDC Code(s): 76176-128-01
- Packager: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
- 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 January 1, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Flammable, keep away from open flame.
When using this product
- avoid contact with eyes. If contact occurs, immediately flush with water.
- using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only once medication should be used, unless directed by a doctor.
- Keep out of reach of children.
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Directions:
- Wash face as you normally would and pat dry with a clean towel.
- Apply a small amount to cotton ball or pad and apply using a dabbing motion.
- Take care to avoid rubbing in eyes.
- Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy.
- Apply a light moisturizer after using astringent.
- If bothersome drying or peeling occurs, reduce application.
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PHARMACYS PRESCRIPTION 8 OZ ACNE CONTROL
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76176-128 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 100 mL Inactive Ingredients Ingredient Name Strength DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) ALCOHOL (UNII: 3K9958V90M) PEG-32 DISTEARATE (UNII: 5730584SOC) DMDM HYDANTOIN (UNII: BYR0546TOW) WATER (UNII: 059QF0KO0R) BENZOPHENONE (UNII: 701M4TTV9O) SODIUM CITRATE (UNII: 1Q73Q2JULR) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHICONE (UNII: 92RU3N3Y1O) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76176-128-01 236.58 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 01/01/2021 Labeler - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098) Registrant - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098) Establishment Name Address ID/FEI Business Operations NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. 530766098 manufacture(76176-128)