Label: BLUE ICE ANALGESIC- menthol gel
- NDC Code(s): 61734-021-01, 61734-021-02, 61734-021-03
- Packager: Delon Laboratories (1990) Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 24, 2023
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- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Delon 8oz (227g)
- Penetro 227g
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INGREDIENTS AND APPEARANCE
BLUE ICE ANALGESIC
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61734-021 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2 g in 100 g Inactive Ingredients Ingredient Name Strength THYMOL (UNII: 3J50XA376E) AMMONIA (UNII: 5138Q19F1X) SODIUM HYDROXIDE (UNII: 55X04QC32I) MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) CARBOMER 934 (UNII: Z135WT9208) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) Product Characteristics Color blue Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61734-021-01 100 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/07/2010 11/06/2017 2 NDC:61734-021-02 113.56 g in 1 CONTAINER; Type 0: Not a Combination Product 05/07/2010 12/04/2014 3 NDC:61734-021-03 227 g in 1 CONTAINER; Type 0: Not a Combination Product 05/07/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/07/2010 Labeler - Delon Laboratories (1990) Ltd (248364184) Establishment Name Address ID/FEI Business Operations Laboratoires Delon 208896216 manufacture(61734-021) , pack(61734-021) , label(61734-021)