Label: MMM TOPICAL ANALGESIC CREAM- methyl salicylate and menthol cream cream
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Contains inactivated NDC Code(s)
NDC Code(s): 69822-030-20 - Packager: Southern Sales & Services, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 September 21, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- DO NOT USE
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WARNINGS
For external use only.
- avoid contact with eyes and mucous membranes
- do not use otherwise than as directed
Caution: Discontinue use if excessive irritation of the skin develops.
When using this product
- do not bandage tightly
- do not apply to wounds or damaged skin.
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again
If pregnant or breast-feeding: ask a health professional before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center Immediately.
- INDICATIONS & USAGE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- MMM Topical Analgesic Cream
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INGREDIENTS AND APPEARANCE
MMM TOPICAL ANALGESIC CREAM
methyl salicylate and menthol cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69822-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 8 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2 g in 100 g Inactive Ingredients Ingredient Name Strength STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CETEARETH-6 (UNII: 2RJS3559D3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69822-030-20 60 g in 1 TUBE; 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 not final part348 01/01/2021 Labeler - Southern Sales & Services, Inc. (013114906) Registrant - Southern Sales & Services, Inc. (013114906)
