![KIEHLS SINCE 1851 SUPERBLY EFFICIENT ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) CREAM [L'OREAL USA PRODUCTS INC]](https://medic.hrt.org//dailymed/images/1252c6dc-c2d5-49b4-9f2a-34c096ee110c/KiehlsSEAP.jpg)
| NDC | 49967-882-01, 49967-882-02 |
| Set ID | 1252c6dc-c2d5-49b4-9f2a-34c096ee110c |
| Category | HUMAN OTC DRUG LABEL |
| Packager | L'Oreal USA Products Inc |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART350 |
- Active ingredient
- Purpose
- Use
- Warnings
- Do not use
- Stop use if
- Ask a doctor before use if
- Keep out of reach of children.
- Directions
-
Inactive ingredients
water, isopropyl myristate, cetyl esters, propylene glycol, PEG-75 stearate, glyceryl stearate, cetyl alcohol, ceteth-20, phenoxyethanol, steareth-20, dimethicone, caprylyl glycol, bisabolol, citrus medica limonum (lemon) fruit extract, hamamelis virginiana (witch hazel) water, hydrolyzed linseed extract, citrus aurantium amara (bitter orange) flower extract, farnesol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 SUPERBLY EFFICIENT ANTIPERSPIRANT AND DEODORANT
aluminum chlorohydrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-882 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 128 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) CETYL ESTERS WAX (UNII: D072FFP9GU) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PEG-75 STEARATE (UNII: OT38R0N74H) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CETYL ALCOHOL (UNII: 936JST6JCN) CETETH-20 (UNII: I835H2IHHX) PHENOXYETHANOL (UNII: HIE492ZZ3T) STEARETH-20 (UNII: L0Q8IK9E08) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL GLYCOL (UNII: 00YIU5438U) LEVOMENOL (UNII: 24WE03BX2T) LEMON (UNII: 24RS0A988O) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) CITRUS AURANTIUM FLOWER (UNII: O730ZX2Z83) FARNESOL (UNII: EB41QIU6JL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-882-01 75 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2010 2 NDC:49967-882-02 50 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 06/01/2010 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 185931458 manufacture(49967-882)
