Home NDC 68828-705 Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on
Product NDC 68828-705
11-digit product format 688280705
Labeler code 68828
Product ID 68828-705_2abdca50-ffcb-8c36-e063-6394a90af766
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Chlorohydrate
Dosage form LIQUID
Route TOPICAL
Labeler Distribuidora Comercial Jafra, S.A. de C.V.
Application M019
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-12-31
Substance ALUMINUM CHLOROHYDRATE
Active strength 12.3 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLOROHYDRATE 12.3 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination HPN8MZW13M Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68828-705-01 Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on 60 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 60 5 68828-705-02 Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on 1 in 1 CARTON LIQUID 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68828-705 JAFRA DAILY SENSITIVE SKIN ANTIPERSPIRANT DEODORANT ROLL-ON (ALUMINUM CHLOROHYDRATE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V.] 5 Current NDC, Legacy NDC, 2 package rows 20250104_0d9b13ff-cd3f-477b-bda4-40e1076584b3.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 70 of 73 · 1,450 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68828-705-01 68828070501 60 mL in 1 BOTTLE, WITH APPLICATOR 60 ml Historical 68828-705-02 68828070502 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68828-705-02) / 60 mL in 1 BOTTLE, WITH APPLICATOR (68828-705-01) 2021-12-31 0000-00-00 No No Current